Bone sialoprotein expression enhances osteoblast differentiation and matrix mineralization in vitro

被引:281
作者
Gordon, Jonathan A. R.
Tye, Coralee E.
Sampaio, Arthur V.
Underhill, T. Michael
Hunter, Graeme K.
Goldberg, Harvey A.
机构
[1] Univ Western Ontario, Schulich Sch Med & Dent, CIHR Grp Skeletal Dev & Remodeling, Dept Biochem, London, ON N6A 5C1, Canada
[2] Univ Western Ontario, Schulich Sch Med & Dent, CIHR Grp Skeletal Dev & Remodeling, Div Oral Biol, London, ON N6A 5C1, Canada
[3] Univ British Columbia, Dept Cellular & Physiol Sci, Vancouver, BC V5Z 1M9, Canada
基金
加拿大健康研究院;
关键词
bone sialoprotein; osteoblasts; noncollagenous proteins; bone mineralization; differentiation;
D O I
10.1016/j.bone.2007.04.191
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Bone sialoprotein (BSP) is air acidic, noncollagenous glycoprotein abundantly expressed in mineralized tissues. Although BSP is frequently used as a marker of osteoblast differentiation, the role of the protein in osteoblast function is unclear. BSP belongs to the SIBLING (Small Integrin-binding LIgand N-linked Glycoprotein) family of RGD-containing matrix proteins, several members of which have been shown to affect cell differentiation. The normal levels of BSP expression in osteoblasts were specifically altered by CMV-mediated adenoviral overexpression in primary osteoblasts or inhibition by an RNA interference-based strategy in the MC3T3E1 cell line. Alternatively, osteoblast cultures were supplemented with recombinant BSP protein. Quantitative real-time PCR was used to monitor the mRNA levels of the osteoblast-related transcription factors Osterix and Runx2 as well as the osteoblast-specific gene osteocalcin. As markers of osteoblast differentiation, alkaline phosphatase enzyme activity, Runx2-luciferase reporter activity and calcein incorporation into mineralized cultures were also measured. The overexpression of BSP increased osteoblast-related gene expression as well as calcium incorporation and nodule formation by osteoblast cultures. Similarly, supplementation of osteoblast cultures with recombinant BSP increased several markers of osteoblast differentiation. Conversely, suppression of BSP expression by small-hairpin RNA-encoding plasmids inhibited expression of osteoblast markers and nodule formation. Overexpression of several functional-domain mutants of BSP demonstrated that increases in osteoblast-related gene expression and matrix mineralization observed in BSP overexpression models are mediated by the integrin-binding RGD motif found near the C-terminus of the protein. These results demonstrate that BSP may serve as a matrix-associated signal directly promoting osteoblast differentiation resulting in the increased production of a mineralized matrix. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:462 / 473
页数:12
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